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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc12a5
solute carrier family 12, member 5
MGI:1862037
64 phenotypes from 6 alleles in 8 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc12a5em1(IMPC)Mbp/Slc12a5+
C57BL/6N-Slc12a5em1(IMPC)Mbp/MbpMmucd
abnormal colon morphology J:211773
abnormal duodenum morphology J:211773
abnormal jejunum morphology J:211773
abnormal placenta morphology J:211773
abnormal skin morphology J:211773
abnormal spleen morphology J:211773
abnormal stomach morphology J:211773
decreased bone mineral content J:211773
embryonic growth retardation J:211773
enlarged spleen J:211773
impaired glucose tolerance J:211773
small spleen J:211773
Slc12a5em1(IMPC)Mbp/Slc12a5em1(IMPC)Mbp
C57BL/6N-Slc12a5em1(IMPC)Mbp/MbpMmucd
abnormal blood vessel morphology J:211773
abnormal placenta morphology J:211773
abnormal placenta vasculature J:211773
edema J:211773
hemorrhage J:211773
microphthalmia J:211773
preweaning lethality, complete penetrance J:211773
Slc12a5tm1Dlp/Slc12a5+
involves: C57BL/6J
abnormal summary potential J:113307
increased susceptibility to pharmacologically induced seizures J:113307
Slc12a5tm1Dlp/Slc12a5tm1Dlp
involves: 129 * C57BL/6J
abnormal brain interneuron morphology J:113307
abnormal gait J:113307
abnormal posture J:113307
abnormal summary potential J:113307
decreased body size J:113307
postnatal growth retardation J:113307
postnatal lethality, complete penetrance J:113307
tonic-clonic seizures J:113307
Slc12a5tm1Hsav/Slc12a5tm1Hsav
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
abnormal nervous system electrophysiology J:127091
Slc12a5tm1Hsav/Slc12a5tm2Hsav
involves: 129S1/Sv * 129S2/SvPasHsd * 129X1/SvJ * C57BL/6J * C57BL/6JOlaHsd
abnormal habituation J:101079
decreased body weight J:101079
decreased vertical activity J:101079
hyporesponsive to tactile stimuli J:101079
impaired spatial learning J:101079
increased anxiety-related response J:101079
increased susceptibility to pharmacologically induced seizures J:101079
increased thermal nociceptive threshold J:101079
normal nervous system phenotype J:101079
normal reproductive system phenotype J:101079
Slc12a5tm1Hsav/Slc12a5tm2Hsav
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
abnormal dendritic spine morphology J:136887
Slc12a5tm1Tjj/Slc12a5tm1Tjj
either: 129X1/SvJ or (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * NMRI)
abnormal abdominal wall morphology J:69625
abnormal action potential J:69625
abnormal central pattern generator function J:69625
abnormal motor capabilities/coordination/movement J:69625
abnormal nervous system electrophysiology J:69625
abnormal somatic nervous system physiology J:69625
abnormal touch/ nociception J:69625
akinesia J:69625
atelectasis J:69625
neonatal lethality, complete penetrance J:69625
omphalocele J:69625
respiratory failure J:69625
trunk curl J:69625
Slc12a5tm2.1Tjj/Slc12a5tm2.1Tjj
Gabra6tm2(cre)Wwis/Gabra6+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal action potential J:181930
abnormal cerebellar granule cell morphology J:181930
abnormal learning/memory/conditioning J:181930
abnormal neuron morphology J:181930
normal behavior/neurological phenotype J:181930
normal nervous system phenotype J:181930
Slc12a5tm2.1Tjj/Slc12a5tm2.1Tjj
Gabra6tm2(cre)Wwis/Gabra6+
Tg(Pcp2-cre)2Mpin/0
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal GABA-mediated receptor currents J:181930
abnormal learning/memory/conditioning J:181930
abnormal motor learning J:181930
abnormal optokinetic reflex J:181930
abnormal vestibuloocular dark reflex J:181930
abnormal vestibuloocular light reflex J:181930
normal nervous system phenotype J:181930
Slc12a5tm2.1Tjj/Slc12a5tm2.1Tjj
Tg(Pcp2-cre)2Mpin/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal GABA-mediated receptor currents J:181930
abnormal learning/memory/conditioning J:181930
abnormal motor learning J:181930
abnormal neuron morphology J:181930
abnormal optokinetic reflex J:181930
abnormal Purkinje cell morphology J:181930
impaired ability to fire action potentials J:181930
normal nervous system phenotype J:181930
normal vision/eye phenotype J:181930
Slc12a5tm2Hsav/Slc12a5tm2Hsav
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
abnormal dendritic spine morphology J:136887
abnormal miniature excitatory postsynaptic currents J:136887
abnormal synapse morphology J:136887

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory